Taiwan FDA registration b0d0397f30cb7160e0e71c82dab6f2f6

"Hua Sheng" ENT Examination and Treatment Table (Unsterilized)

TW: "華陞" 耳鼻喉檢查及治療台 (未滅菌)

Taiwan·Risk Class 1·HUA SHENG INSTRUMENTS CO., LTD.·Registered Nov 08, 2010 – Nov 08, 2025Expired

Registration details

Analysis ID: b0d0397f30cb7160e0e71c82dab6f2f6

Company information

Manufacturer: HUA SHENG INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HUA SHENG INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "ENT Examination and Treatment Unit (G.5300)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5300 ENT examination and treatment table
Import Information: Domestic

Dates and status

Registration Date: Nov 08, 2010
Expiry Date: Nov 08, 2025

About this record

Access comprehensive regulatory information for "Hua Sheng" ENT Examination and Treatment Table (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0d0397f30cb7160e0e71c82dab6f2f6 and manufactured by HUA SHENG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HUA SHENG INSTRUMENTS CO., LTD..

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